A systematic review of FOLFOXIRI chemotherapy for the first-line treatment of metastatic colorectal cancer: improved efficacy at the cost of increased toxicity
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作者:
Montagnani, F.
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S Giuseppe Hosp, Dept Oncol, Oncol Unit, Florence, ItalyS Giuseppe Hosp, Dept Oncol, Oncol Unit, Florence, Italy
Montagnani, F.
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Chiriatti, A.
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Univ Siena, Sch Med, Nurse Med Sch, I-53100 Siena, ItalyS Giuseppe Hosp, Dept Oncol, Oncol Unit, Florence, Italy
Chiriatti, A.
[2
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Turrisi, G.
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机构:S Giuseppe Hosp, Dept Oncol, Oncol Unit, Florence, Italy
Turrisi, G.
Francini, G.
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Univ Siena, Sch Med, Med Oncol Unit, Giorgio Segre Dept Pharmacol, I-53100 Siena, ItalyS Giuseppe Hosp, Dept Oncol, Oncol Unit, Florence, Italy
Francini, G.
[3
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Fiorentini, G.
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机构:S Giuseppe Hosp, Dept Oncol, Oncol Unit, Florence, Italy
Fiorentini, G.
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[1] S Giuseppe Hosp, Dept Oncol, Oncol Unit, Florence, Italy
Aim The simultaneous administration of irinotecan, 5-fluorouracil, folinic acid and oxaliplatin (FOLFOXIRI) has been compared with standard 5-fluorouracil, folinic acid and irinotecan (FOLFIRI) in randomized trials in metastatic colorectal cancer patients. A superior efficacy of FOLFOXIRI has been reported by some authors, but others have failed to show any differences and do not recommend its use because of greater cost and toxicity. We performed a systematic review of the literature to analyse efficacy and toxicity of FOLFOXIRI. Method Odds ratios (OR) with 95% confidence intervals (CI) were used to analyse dichotomous variables. Hazard ratios (HR) for progression and death were combined with an inverse variance method based on logarithmic conversion. A fixed-effect model and Mantel-Haenszel's method were used. Heterogeneity was tested with Cochrane's Q test and I-2 test. Results A significant increase in response rate (OR 2.04; P < 0.01) was associated with treatment by FOLFOXIRI and a benefit was also shown by the HR for progression (HR 0.72; P < 0.01) and death (HR 0.71; P < 0.01). Analysis for toxicity found a significant increase associated with FOLFOXIRI except for anaemia, fatigue and febrile neutropenia. Conclusion FOLFOXIRI confers significant benefit in progression-free survival, survival, response and R0 resection rates but is more toxic compared with FOLFIRI.
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King Faisal Specialist Hosp & Res Ctr, Oncol Ctr, POB 3354, Riyadh 11211, Saudi ArabiaKing Faisal Specialist Hosp & Res Ctr, Oncol Ctr, POB 3354, Riyadh 11211, Saudi Arabia
Bazarbashi, S.
Hakoun, A. M.
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Alfaisal Univ, Coll Med, Res Off, Riyadh, Saudi ArabiaKing Faisal Specialist Hosp & Res Ctr, Oncol Ctr, POB 3354, Riyadh 11211, Saudi Arabia
Hakoun, A. M.
Gad, A. M.
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King Faisal Specialist Hosp & Res Ctr, Oncol Ctr, POB 3354, Riyadh 11211, Saudi Arabia
Ain Shams Univ, Fac Med, Clin Oncol & Nucl Med Dept, Cairo, EgyptKing Faisal Specialist Hosp & Res Ctr, Oncol Ctr, POB 3354, Riyadh 11211, Saudi Arabia
Gad, A. M.
Elshenawy, M. A.
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King Faisal Specialist Hosp & Res Ctr, Oncol Ctr, POB 3354, Riyadh 11211, Saudi Arabia
Menoufia Univ, Clin Oncol & Nucl Med Dept, Fac Med, Shibin Al Kawm, EgyptKing Faisal Specialist Hosp & Res Ctr, Oncol Ctr, POB 3354, Riyadh 11211, Saudi Arabia
Elshenawy, M. A.
Aljubran, A.
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King Faisal Specialist Hosp & Res Ctr, Oncol Ctr, POB 3354, Riyadh 11211, Saudi ArabiaKing Faisal Specialist Hosp & Res Ctr, Oncol Ctr, POB 3354, Riyadh 11211, Saudi Arabia
Aljubran, A.
Alzahrani, A. M.
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King Faisal Specialist Hosp & Res Ctr, Oncol Ctr, POB 3354, Riyadh 11211, Saudi ArabiaKing Faisal Specialist Hosp & Res Ctr, Oncol Ctr, POB 3354, Riyadh 11211, Saudi Arabia
Alzahrani, A. M.
Eldali, A.
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King Faisal Specialist Hosp & Res Ctr, Res Ctr, Dept Biostat Epidemiol & Sci Comp, Riyadh, Saudi ArabiaKing Faisal Specialist Hosp & Res Ctr, Oncol Ctr, POB 3354, Riyadh 11211, Saudi Arabia